FDA Inspection 1098055 — Fitrite Incorporated
The FDA completed an inspection of Fitrite Incorporated on July 31, 2019 in Quezon City. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Food/Cosmetics.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- July 31, 2019
- Fiscal Year
- 2019
- Product Type
- Food/Cosmetics
- Project Area
- Food Composition, Standards, Labeling and Econ
- Location
- Quezon City (Philippines)
Citations
| ID | CFR | Description |
|---|---|---|
| 12747 | 21 CFR 120.8(b)(3) | HACCP plan - critical limits not listed or not adequate |
| 18145 | 21 CFR 117.35(c) | Pest control |
| 9954 | 21 CFR 120.11(a)(1)(iv) | Verification - CCP, CA record review |